EP1366811B1

EP1366811B1 - Oxysulfide photocatalyst for use in decomposition of water by visible light

Info

Publication number: EP1366811B1
Application number: EP02711218A
Authority: EP
Inventors: Kazunari Domen; Michikazu Hara; Tsuyoshi Takata; Akio Ishikawa
Original assignee: Japan Science and Technology Agency
Current assignee: Japan Science and Technology Agency
Priority date: 2001-02-07
Filing date: 2002-01-23
Publication date: 2007-09-19
Anticipated expiration: 2022-01-23
Also published as: WO2002062467A1; US20040029726A1; JP2002233770A; US6838413B2; DE60222534D1; EP1366811A1; DE60222534T2; JP4107807B2; EP1366811A4

Description

FIELD OF THE INVENTION

The present invention relates to a novel photocatalyst. Namely, this invention relates to a visible light active photocatalyst comprising oxysulfide which contains at least one transition metal, and also relates to a photocatalyst for water-splitting.

BACKGROUND OF THE INVENTION

The following photocatalytic reaction is well-known as a technique to obtain the intended subject. That is, light is irradiated to solid compound which has a photocatalytic function so as to generate excited electrons and holes. Then a substance is oxidized or reduced by said excited electrons and holes to obtain the desired object.
In particular, photocatalytic decomposition of water, is interesting from the view point of solar energy conversion. Further, a photocatalyst which shows activity in the photocatalytic decomposition of water can be recognized as an excellent photo functional material which provides functions such as photo absorption, electrolytic separation or oxidation-reduction reaction at the surface.
Kudo, Kato et al, are explaining that alkaline tantalate or alkaline earth element is a photocatalyst which shows excellent activity in the stoichiometric photocatalytic decomposition of water by quoting various prior arts [for example, Catal. Lett., 58 (1999), 153-155; Chem. Lett., (1999), 1207; Surface, Vol.36, No.12 (1998), 625-645 (hereinafter shortened to Document A)] . In the above Document A, there is an explanation of useful photocatalytic materials for proceeding the decomposing reaction of water to hydrogen and/or oxygen using a photocatalyst, and many indications about photocatalysts used for stoichiometric photocatalytic decomposition of water are mentioned. Further, a photocatalyst which loads a promoter such as platinum or NiO is referred.
However, only metal oxides are used as photocatalysts in Document A. And in the cases of various solid photocatalysts, since the width of a forbidden band exists between a valence electron band and a conduction band, that is, band gap energy is large (>3eV), it is difficult to excite it by low energy (energy: under 3eV). On the contrary, almost all of the conventional solid photocatalysts which can generate electrons or holes by visible-light radiation are unstable under the conditions of a photo-catalytic water decomposing reaction. For example, the band gap energy of CdS or Cu-ZnS is 2.4eV, but the catalytic reaction is restricted because it is affected by photo-corrosive action, which is corrosive oxidative action. In the meanwhile, almost all of the solar light which reaches the surface of the earth is visible light radiation of lower energy. Therefore, for the purpose of progressing the various photo-catalytic reactions effectively, a stable photocatalyst which acts by visible light is needed. However, among the conventional techniques, there is no technique to satisfy the above requirement.
As shown in Fig. 5, the U.V.(ultra violet) visible light diffuse reflectance spectrum of cadmium sulfide CdS on the market (99.99% purity) is measured and it become clear that it absorbs the light of spectrum region from ultra violet to visible light of 550nm. Further, according to the reports of many researchers, in the case of CdS, since a valence electron band and a conduction band, which form band gap 2.4eV, has surplus to generate oxygen and hydrogen by electric potential view, theoretically it is deemed to have an ability to decompose water to hydrogen and oxygen. However, there is a report which reports that when decomposing reaction of water is carried out by irradiating visible light over 440nm, hydrogen can be obtained in a stable form but the generation of oxygen cannot be observed at all. This phenomenon can be explained as follows. That is, photo dissolution of the catalyst itself (photo-corrosive action) is caused because of poor stability of chemical species on the catalyst surface and when a positive hole in the inside of the solid caused by photo excitation is transferred to the surface, it oxidizes a S^2- on the surface prior to a water molecule and forms a surface film.
From the above fact, it is obviously known that the pure sulfide CdS can reduce protons to hydrogen by visible light having a longer wavelength than 440nm, but it is not a particularly stable material against nascent oxygen so as to generate oxygen from water, and does not have such ability.
The inventors of the present invention have conjectured that, since a valence electron of a nitrogen atom has higher energy than that of an oxygen atom, the band gap energy of metal compound containing nitrogen atom can be made smaller than that of metal oxide, and when a metal and a metal compound are bonded with an adequate amount of nitrogen atoms it becomes possible to generate excited electrons and holes and to provide a photocatalyst which acts by visible light irradiation. The inventor of the present invention synthesized an oxynitride containing a transition metal and proposed a photocatalyst which acts by visible light (refer to JP Application No. 2000-256681 ).
Still more, since a valence band of numerous sulfides is originated to S 3P orbit and is locating at negative electric potential compared with an O2p orbit of oxide, a sulfide is known as an advantageous material to accomplish the visible light absorption.
The object of the present invention is to provide a novel photocatalyst which can generate hydrogen and oxygen from water in a stable maner by visible light irradiation. In the meanwhile, as mentioned above, valence bands of numerous sulfides are located at more negative potentials compared to those of oxides, and it is possible to conjecture that the numerous sulfides improve the characteristics of visible light absorption. Therefore the inventors of the present invention, considered that when a metal and a metal compound which are bonded with adequate amount of sulfur atoms, it becomes possible to generate excited electrons and holes by absorption of visible light of longer wave length, and it will be possible to produce a photocatalyst which acts by visible light. Accordingly, the inventors of the present invention synthesized a compound in which an oxide of transition metal and a transition metal bonded with adequate amount of sulfur atoms are existing and the photo-catalytic characteristics of the compound are investigated, and have found that the compound acts as a photocatalyst which can generate both hydrogen and oxygen by photo decomposition of water under the presence of a sacrificial catalyst. Thus, the inventors of the present invention have accomplished the present invention.
The invention provides a photocatalyst comprising an oxysulfide which comprises at least one transition metal chosen from titanium and niobium, and the photocatalyst further comprises a rare earth element chosen from samarium and lanthanum, wherein the photocatalyst has loaded thereon a promoter chosen from nickel oxide and platinum. The invention further provides photocatalyst for use in photodecomposition of water. The invention further provides use of an oxysulfide which comprises at least one transition metal chosen from titanium and niobium and a rare earth element chosen from samarium and lanthanum, and having loaded thereon a promoter chosen from nickel oxide and platinum, as a photocatalyst.

BRIEF ILLUSTRATION OF THE DRAWINGS

Figure 1 shows X-ray diffraction pattern of calcined Sm₂Ti₂O₅S₂ according to the producing condition of Sm₂Ti₂O₅S₂ of Example 1.
Figure 2 shows U.V.·visible light diffuse reflectance spectrum of calcined Sm₂ Ti₂O₅S₂ according to the producing condition of Sm₂Ti₂O₅S₂ of Example 1.
Figure 3 shows hydrogen evolution rate by suspending 0.2 g of "1 wt% Pt promoter being loaded on Sm₂Ti₂O₅S₂", which is a photocatalyst of Example 1, into 0.200dm^-3 of aqueous solution of 10 vol% methanol and irradiating the visible light longer than 440nm wavelength.
Figure 4 shows oxygen evolution rate by suspending 0.2 g of "1 wt% Pt promoter being loaded on Sm₂ Ti₂O₅S₂", which is a photocatalyst of Example 1, into aqueous solution of 0.01 mol dm^-3 AgNO₃ and irradiating the visible light longer than 440 nm wavelength.
Figure 5 shows the U.V.-visible light diffuse reflectance spectrum of cadmium sulfide CdS (99.99% purity) on the market.
Fig.6 shows the U.V. visible light diffuse reflectance spectrum of titanium oxide TiO₂ (99.99% purity) on the market.

The present invention will be illustrated more in details.

A. The photocatalyst of the present invention can be obtained by following process. That is, oxide or sulfide of rare earth and oxide or sulfide of transition metal are mixed together with by desired mixing amount and contained into a sealed tube which does not cause a problem of contamination, for example, a quartz tube or a niobium tube. After vacuum sealed, calcined by adjusting the temperature elevating speed including maintaining the temperature at constant temperature and heating time.
The rare earth oxide is samarium oxide (Sm₂O₃) or lanthanum oxide (La₂O₃) and the rare earth sulfide is samarium sulfide (Sm₂S₃) or lanthanum sulfide (La₂S₃). The transition metal oxide is titanium oxide (TiO₂) or niobium oxide (Nb₂O₅) and the transition metal sulfide is titanium sulfide (TiS₂ or niobium sulfide (Nb₂S₅).
B. The catalytic activity of the oxysulfide compound containing transition metal obtained by the above calcination process is improved by providing a promoter.
The promoter is platinum (Pt) or Nickel oxide (NiO). The amount of the promoter to be provided to the catalyst is suitably from 0.1 to 10 wt%.

As the method to provide the promoter, a conventional providing method of a promoter to a photocatalyst can be used. For example, in the case of Pt, aqueous solution of tetraaminedichloroplatinum [Pt(NH₃)₄Cl₂] is penetrated into catalyst and dried, then reduced by hydrogen, thus Pt can be added.

EXAMPLES

The present invention will be illustrated more in details according to the Example. However, the following Examples are mentioned for the purpose to clearly explain the usefulness of the present invention and not to intending to limit the scope of the present invention.

Example 1

To produce 5g of Sm₂Ti₂O₅S₂, samarium sulfide (Sm₂S₃), titanium oxide (TiO₂) and titanium sulfide (TiS₂) are mixed together with by 1:1:1 ratio and contained into a quartz tube. After vacuum sealing the quartz tube, the calcinating process is carried out by following condition. The temperature is elevated from the room temperature to 400°C by 15°C/1hr elevating speed and maintain the temperature of 400°C for 24hours. After that, the temperature is elevated to 1000°C by 20°C/1hr elevating speed and maintain said temperature for 7 days. Then the temperature is cooled down to the room temperature by 30°C/1hr cooling speed, and the aimed product is obtained.

Loading of Pt promoter

The corresponding amount of tetraamminedichloroplatinum Pt(NH₃)₄Cl₂ to 1wt% of the catalyst is impregnated onto the catalyst in aqueous solution and dried on a water bath, then reduced by hydrogen at 573K for 2 hours.
The X-ray diffraction pattern after calcination is shown in Fig.1. All diffraction peaks in the graph are assigned to those of Sm₂Ti₂O₅S₂, and the generation of Sm₂Ti₂O₅S₂ is confirmed.
U.V. visible light diffuse reflectance spectrum of the above material is shown in Fig.2. According to Fig.2, it becomes clear that said material absorbs the light of wavelength shorter than 650nm.
Fig.3 shows hydrogen evolution rate by suspending 0.2g of 1 wt% Pt promoter loaded material into 0.200dm^-3 of aqueous solution of 10 vol% methanol and irradiating the visible light of wavelength longer than 440nm. As the light source, a xenon lamp of 500W is used, and visible light of longer wavelength than 440nm is irradiated by using a wavelength filter which cut off the light of shorter wavelength than 440nm. As shown in Fig.3, it become clear that the above catalyst can generate hydrogen constantly from aqueous solution of methanol under the irradiation of visible light of longer wavelength than 440nm. 0.2g of said material is suspended in aqueous solution of 0.01mol dm^-3 AgNO₃, the visible light of longer wavelength than 440nm is irradiated, and oxygen evolution rate is shown in Fig.4. The reaction is carried out by the same condition. It becomes clear that said material can generate oxygen from aqueous solution of silver nitrate under the irradiation of visible light longer than 440nm wavelength. As mentioned above, it is recognized that Sm₂Ti₂O₅S₂ has an ability to reduce protons to hydrogen and to oxidize water to oxygen by the visible light of longer wavelength than 440nm.

Comparative Example 1

In this Comparative Example, cadmium sulfide (99.99% purity) on the market is used. Same to the Example 1, the reaction is carried out under the irradiation of the visible light longer than 440nm wavelength, and the results of experiments of hydrogen generation and oxygen generation are illustrated.

The results show that although hydrogen is generated stably, the generation of oxygen is not observed. That is, pure cadmium sulfide CdS can reduce a proton to hydrogen by visible light of longer than 440nm wave length, however, is not a so stable material to generate oxygen from water.

Comparative Example 2

In this Comparative Example, the photo catalytic characteristics of titanium dioxide TiO₂ on the market is explained for the comparison with the present invention. Fig.6 shows that the diffuse reflectance spectrum of said titanium dioxide TiO₂ is shorter than 420nm. Therefore, in the reaction using light (U.V. light) which can be absorbed, it is understood that TiO₂ has an ability to decompose water to hydrogen and oxygen.

However, it is a matter of cause, under the irradiation of visible light longer than 440nm, the generation of hydrogen and oxygen is not observed.

In the above Example 1, the case in which Ti is used as a transition metal is explained, however, the similar result can be obtained when Nb, which is a transition metal usually used in the field of photocatalyst, is used.

INDUSTRIAL APPLICABILITY

As mentioned above, the photocatalyst obtained by the present invention, is the catalyst that acts by visible light shorter than 650nm wavelength, which is the majority in solar light reaching to the surface of the earth. By carrying out the photocatalyst reaction with solar light, the useful compound can be produced. Further, as indicated in Examples, since said photocatalyst has an ability to decompose water to hydrogen and oxygen by visible light radiation, it is hopeful to be used as a photocatalyst which converts solar light to hydrogen being considered as the energy of next generation.

Claims

A photocatalyst comprising an oxysulfide which comprises at least one transition metal chosen from titanium and niobium, and the photocatalyst further comprises a rare earth element chosen from samarium and lanthanum, wherein the photocatalyst has loaded thereon a promoter chosen from nickel oxide and platinum.
Use of an oxysulfide which comprises at least one transition metal chosen from titanium and niobium and a rare earth element chosen from samarium and lanthanum, and having loaded thereon a promoter chosen from nickel oxide and platinum, as a photocatalyst.
A process for photodecomposition of water, comprising the use of a photocatalyst according to claim 1.